QC Microbiology Supervisor

About the role

The QC Microbiology Supervisor oversees daily Quality Control Microbiology activities, ensures all testing/data review is completed within appropriate timeframes, delivers daily expectations and assignments, provides in-lab support, as needed, and oversight of routine/on-demand testing. They provide coaching and feedback to Quality Control microbiology team, participate in Quality Control deviation investigations, laboratory investigations and CAPA implementation, influence the accomplishments of companywide and team goals and objectives, and inspire team members while consistently modeling ALP values in all interactions.

This individual ensures all work is carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs). They constantly evaluate internal processes and procedures and work to create a productive space while maintaining the highest possible quality standards.

Essential Job Functions

• Provide technical support, oversight and team leadership for Quality Control Microbiology
• Assist in the development of individual team members by providing mentorship to analysts/data reviewers and communicating with Quality Control Leadership on team performance
• Develop and improve current processes to maintain and control the general functions of INCOG Quality Control
• Assure compliance with cGMP requirements (current good manufacturing practices)
• Perform laboratory walk-throughs and ensure laboratory spaces maintain inspection readiness and control

Special Job Requirements

• Knowledge of Quality Control Microbiology, GxP principles, CAPA/Investigation management, and data/document review
• Familiarity with relevant quality and regulatory requirements and trends and cGMP's
• Strong communication skills and the ability to build relationships with colleagues across all levels of the organization, including business managers, operations leaders, and technical leaders
• Knowledge of Aseptic techniques and processing

Additional Preferences

• 3-5 years demonstrated working knowledge of GMP laboratory operations
• 1-2 years in a people leadership role

Benefits

INCOG BioPharma Services is a smoke-free campus. INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. Qualified applicants must be authorized to work in the United States on a full-time basis.

All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate.

We will not tolerate discrimination or harassment based on any of these characteristics. Qualified applicants must be authorized to work in the United States on a full-time basis. INCOG will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.